<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7</volume><submitter>Kelliher T</submitter><pubmed_abstract>Doubled haploid plants are invaluable breeding tools but many crop species are recalcitrant to available haploid induction techniques. To test if haploid inducer lines can be engineered into crops, CENH3 (-∕-) and CENH3:RNAi lines were complemented by AcGREEN-tailswap-CENH3 or AcGREEN-CENH3 transgenes. Haploid induction rates were determined following testcrosses to wild-type plants after independently controlling for inducer parent sex and transgene zygosity. CENH3 fusion proteins were localized to centromeres and did not cause vegetative defects or male sterility. CENH3:RNAi lines did not demonstrate consistent knockdown and rarely produced haploids. In contrast, many of the complemented CENH3 (-∕-) lines produced haploids at low frequencies. The rate of gynogenic haploid induction reached a maximum of 3.6% in several hemizygous individuals when backcrossed as males. These results demonstrate that CENH3-tailswap transgenes can be used to engineer in vivo haploid induction systems into maize plants.</pubmed_abstract><journal>Frontiers in plant science</journal><pagination>414</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4814585</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Maternal Haploids Are Preferentially Induced by CENH3-tailswap Transgenic Complementation in Maize.</pubmed_title><pmcid>PMC4814585</pmcid><pubmed_authors>Kelliher T</pubmed_authors><pubmed_authors>Nuccio ML</pubmed_authors><pubmed_authors>Starr D</pubmed_authors><pubmed_authors>Wang W</pubmed_authors><pubmed_authors>Zhong H</pubmed_authors><pubmed_authors>McCuiston J</pubmed_authors><pubmed_authors>Martin B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Maternal Haploids Are Preferentially Induced by CENH3-tailswap Transgenic Complementation in Maize.</name><description>Doubled haploid plants are invaluable breeding tools but many crop species are recalcitrant to available haploid induction techniques. To test if haploid inducer lines can be engineered into crops, CENH3 (-∕-) and CENH3:RNAi lines were complemented by AcGREEN-tailswap-CENH3 or AcGREEN-CENH3 transgenes. Haploid induction rates were determined following testcrosses to wild-type plants after independently controlling for inducer parent sex and transgene zygosity. CENH3 fusion proteins were localized to centromeres and did not cause vegetative defects or male sterility. CENH3:RNAi lines did not demonstrate consistent knockdown and rarely produced haploids. In contrast, many of the complemented CENH3 (-∕-) lines produced haploids at low frequencies. The rate of gynogenic haploid induction reached a maximum of 3.6% in several hemizygous individuals when backcrossed as males. These results demonstrate that CENH3-tailswap transgenes can be used to engineer in vivo haploid induction systems into maize plants.</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016</publication><modification>2024-11-20T18:20:43.778Z</modification><creation>2019-03-27T03:10:43Z</creation></dates><accession>S-EPMC4814585</accession><cross_references><pubmed>27066050</pubmed><doi>10.3389/fpls.2016.00414</doi></cross_references></HashMap>